Run ID: SRR7796667
Sample name:
Date: 04-04-2023 20:20:46
Number of reads: 564863
Percentage reads mapped: 70.65
Strain: lineage2.2.2
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.99 |
lineage2.2.2 | East-Asian (Beijing) | Beijing-RD105/RD207 | RD105;RD207 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.96 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289214 | p.Gln10* | stop_gained | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326110 | p.Trp455* | stop_gained | 0.13 | ethionamide |
ethA | 4326130 | c.1343delA | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7173 | p.Asp645Val | missense_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760111 | p.Ser102Phe | missense_variant | 0.15 |
rpoC | 762632 | c.-738C>T | upstream_gene_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764616 | p.Asn416Ser | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 778743 | p.Val55Met | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781406 | c.-154_-153insC | upstream_gene_variant | 1.0 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.1 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.11 |
Rv1258c | 1406377 | p.Gly322Ser | missense_variant | 0.14 |
embR | 1416693 | p.Asp219Asn | missense_variant | 0.14 |
atpE | 1461282 | p.Val80Ile | missense_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473492 | n.-166T>C | upstream_gene_variant | 0.11 |
rrl | 1474887 | n.1230T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475578 | n.1921C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1673406 | c.-796C>T | upstream_gene_variant | 1.0 |
rpsA | 1833909 | p.Asp123Ala | missense_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834927 | c.1386A>G | synonymous_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918485 | c.546G>A | synonymous_variant | 0.12 |
katG | 2154014 | p.Ser700Thr | missense_variant | 0.1 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155068 | c.1044T>A | synonymous_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168801 | c.1812A>G | synonymous_variant | 0.11 |
PPE35 | 2169202 | p.Ser471Pro | missense_variant | 0.11 |
PPE35 | 2170024 | p.Thr197Ser | missense_variant | 0.2 |
Rv1979c | 2223195 | c.-32delT | upstream_gene_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290079 | c.-838T>A | upstream_gene_variant | 0.11 |
kasA | 2517975 | c.-140A>T | upstream_gene_variant | 0.1 |
ahpC | 2726245 | p.Leu18His | missense_variant | 0.11 |
ahpC | 2726684 | c.492G>A | synonymous_variant | 0.11 |
ribD | 2986828 | c.-11C>T | upstream_gene_variant | 0.11 |
thyA | 3073867 | p.Thr202Ile | missense_variant | 0.1 |
thyA | 3074122 | p.Asp117Gly | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474225 | c.219C>T | synonymous_variant | 0.2 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
clpC1 | 4038364 | p.Ile781Phe | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4246085 | p.Glu951Asp | missense_variant | 0.13 |
embB | 4246583 | p.Arg24Cys | missense_variant | 0.4 |
aftB | 4267203 | p.Lys545Arg | missense_variant | 0.11 |
aftB | 4267419 | p.Ala473Val | missense_variant | 0.11 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268394 | p.Leu148Pro | missense_variant | 0.14 |
ubiA | 4269784 | p.Val17Glu | missense_variant | 0.1 |
ubiA | 4269911 | c.-78G>A | upstream_gene_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |